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Updated: Jul 31, 2025

Quantification of Monocyte Transmigration and Foam Cell Formation from Individuals with Chronic Inflammatory Conditions
Published on: October 17, 2017
Monocyte heterogeneity in cardiovascular disease
Adele V Ruder1, Suzan M W Wetzels1, Lieve Temmerman1
1Department of Pathology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC+), P. Debyelaan 25, 6229 HX Maastricht, The Netherlands.
Monocyte subsets, including intermediate monocytes (intMo), are linked to cardiovascular disease (CVD). Further research is needed to understand their functional roles and improve CVD prediction and treatment strategies.
Area of Science:
- Immunology
- Cardiovascular Biology
- Cellular Heterogeneity
Background:
- Monocytes are key immune cells differentiating into macrophages (MФ), playing roles in cardiovascular disease (CVD) pathogenesis.
- Current monocyte classification into classical (cMo), intermediate (intMo), and non-classical (ncMo) subsets based on CD14 and CD16 expression shows altered distributions in CVD.
- The causal role and predictive value of specific monocyte subsets in CVD remain unclear, despite associations with conditions like atherosclerosis and heart failure.
Purpose of the Study:
- To review current knowledge on monocyte heterogeneity in homeostasis and disease, particularly in the context of CVD.
- To explore the functional differences between macrophage (MФ) populations derived from distinct monocyte subsets.
- To highlight the implications of monocyte subset heterogeneity for cardiovascular health and disease.
Main Methods:
- Literature review of recent high-parameter cytometry and single-cell RNA sequencing (scRNA-Seq) studies.
- Analysis of existing data on monocyte subset distribution in cardiovascular disease.
- Synthesis of findings on monocyte-derived macrophage (MФ) functionality.
Main Results:
- Monocyte subsets exhibit significant heterogeneity, with intermediate monocytes (intMo) frequently associated with CVD.
- Emerging evidence suggests functional disparities between MФ derived from different monocyte subsets.
- Current classification may not fully capture the complexity of monocyte heterogeneity and its role in CVD.
Conclusions:
- Understanding the functional diversity of monocyte subsets is crucial for elucidating their role in CVD pathogenesis.
- An updated nomenclature and further functional studies are necessary to clarify the specific contributions of each monocyte subset to cardiovascular disease.
- Targeting specific monocyte subsets or their differentiated MФ populations may offer novel therapeutic strategies for CVD.
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